Incidence of Perioperative Hypothermia in Patients With Elective Surgery Under General Anesthesia in Turkey (GAPOHI)

April 12, 2016 updated by: Hulya Bilgin, Turkish Society of Anesthesiology and Reanimation

National Epidemiology Survey on the Incidence of Perioperative Hypothermia in Patients With Elective Surgery Under General Anesthesia in Turkey

Primary objective of the study is to project the incidence rate of perioperative hypothermia under general anesthesia in patients who go under minimum 1 hour long elective surgery in at least 25 hospitals/medical centers in Turkey .

Secondary objectives are to determine the patient risk factors associated with perioperative hypothermia, to determine the surgery risk factors associated with perioperative hypothermia, to determine the other risk factors associated with perioperative hypothermia, intraoperative infusion volume and effect of warming, intraoperative irrigation volume and effect of warming, intraoperative blood infusion volume and effect of warming, to determine complications related to perioperative hypothermia, to improve patient temperature management awareness and processes.

Study Overview

Status

Unknown

Intervention / Treatment

Detailed Description

Mild hypothermia during perioperative period is very common, and the percentage accounts for about half of all patients undergoing operations, which is directly related to the following three major adverse events that significantly increase their risks: 1) cardiac complications, 2) hemorrhage, 3) infection complications , particularly in patients with high risk factors (ASA grade III, IV). Furthermore, the decrease in body temperature may also lead to the following situations: 1) prolongation in retention time in post-anesthetic ICU (PACU), 2) decrease in the thermal comfort for patients, and thus affecting the satisfaction degree of patients and increasing cost.

From the viewpoint of patient safety, body surface temperature is only a vital sign. Therefore, in order to prevent hypothermia during perioperative period, core temperature monitoring must be carried out from the very beginning of the operation. The heat loss during operations should be minimized. Active warming measurements should be taken for high risk patients during the entire procedures of operations.

Although the literature have reported high incidence rate of hypothermia during perioperative period of selective operations, there's no detailed information about perioperative hypothermia prevalence in Turkey. Actually there are only a few studies about patient warming effectiveness. A small scale study done by Kocaeli University in Turkey in 2013 shows the post operative hypothermia incidence as 45.7%. Another study and survey done by Cerrahpasa Medicine Faculty shows even among healthcare professionals there is great variance about the perception and results of hypothermia. Those facts drives investigators to gather more clinical evidence about perioperative hypothermia.

Under the supervision of Turkish Anesthesiology and Reanimation Society and coordination of Prof Dr Hulya Bilgin from Uludag University Medicine Faculty Anesthesiology and Reanimation Clinic it is aimed to gather evidence about hypothermia prevalence patients who go under minimum 1 hour elective surgery under general anesthesia. So with the results of such a study it is aimed to improve the standard protocols regarding patient temperature management, patient warming management and also to avoid the complications and costs related to hypothermia.

In order to further obtain information on the current status of temperature monitoring and perioperative warming practice in most parts of the country, to project incidence rate of perioperative hypothermia in most parts of the country, explore the relationship between perioperative hypothermia and postoperative clinical outcome, and to provide evidence for the improvement of perioperative body temperature management guidelines in accordance with characteristics of the current Turkish healthcare status, investigators will conduct surveys in department of anesthesiology over certain regions of Turkey to carry out a large scale prospective study. In the study, investigators will search the incidence rate of perioperative hypothermia in the surveyed areas, explore the causes of hypothermia, base on which it is expected to enable to project perioperative hypothermia incidence rate, to verify the effectiveness of perioperative hypothermia risk assessment questionnaire for patients under general anesthesia, and to provide guidance and evidence for the clinical practice of perioperative warming care.

Study Type

Observational

Enrollment (Anticipated)

3000

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years to 88 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Patients undergoing elective surgery under general anesthesia.

Description

Inclusion Criteria:

  • Male or female, ≥18 years old
  • Subject will undergo an elective surgery under general anesthesia
  • The duration of surgery is expected to be over 60 minutes
  • Patients or relatives whom the study is explained and their informed consent is documented
  • Patients who are preplanned to be in ICU after surgery will not be excluded

Exclusion Criteria:

  • Central high fever caused by enter nerves system disease or condition, including that induced by cerebrovascular disease, cerebral trauma, cerebral surgeries, epilepsy and acute hydrocephalus
  • Thermoregulation abnormalities including malignant hyperthermia (MHS) and neuroleptic malignant syndrome, hypothyroidism or hyperthyroidism diagnosed by substantial evidence
  • Infectious fever
  • Temperature is higher than 37.8 Celcius degree within 3 days before surgery
  • Diseases or that may lead to inaccuracy in measurement, such as ear infection
  • Therapeutic preoperative hypothermia
  • Trauma related bleeding, shock and extensive fluid resuscitating surgeries
  • Acute or chronic spine injury cases

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
The incidence rate of perioperative hypothermia in Turkey
Time Frame: 2 months
2 months

Secondary Outcome Measures

Outcome Measure
Time Frame
The patient risk factors associated with perioperative hypothermia.
Time Frame: 2 months
2 months
The surgery risk factors associated with perioperative hypothermia.
Time Frame: 2 months
2 months
Complications related to perioperative hypothermia
Time Frame: 2 months
2 months
Patient temperature management development strategies
Time Frame: 2 months
2 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Hulya Bilgin, Prof, Turkish Society of Anesthesiology and Reanimation

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

March 1, 2016

Primary Completion (Actual)

April 1, 2016

Study Completion (Anticipated)

June 1, 2016

Study Registration Dates

First Submitted

April 1, 2016

First Submitted That Met QC Criteria

April 12, 2016

First Posted (Estimate)

April 13, 2016

Study Record Updates

Last Update Posted (Estimate)

April 13, 2016

Last Update Submitted That Met QC Criteria

April 12, 2016

Last Verified

April 1, 2016

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • TurkishARD

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Yes

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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